Testing 50 mg Usnoflast against a placebo for amyotrophic lateral sclerosis (ALS)

Exclusion

• −Known allergy, sensitivity, or intolerance to Investigational product or excipients.
• −Subjects with Human immunodeficiency virus, hepatitis B, hepatitis C, coronary artery disease, or active gastrointestinal condition that might interfere with drug absorption.
• −Presence of unstable psychiatric disease, cognitive impairment, dementia, or substance abuse that would impair the ability of the subject to provide informed consentInformed consentThe process of being told what taking part involves, then choosing freely.Read more →, in the opinion of the investigatorPrincipal investigatorThe doctor or researcher responsible for running the study at a site.Read more →.
• −Serious illness (e.g., pneumonia, septicemia) within 4 weeks of the screening visitScreeningThe checks done before joining, to see whether a study fits.Read more →; infection requiring hospitalization or treatment with intravenous antibiotics, antivirals, or antifungals within 4 weeks of screening; chronic bacterial infection (such as tuberculosis) deemed unacceptable as per the judgment of the investigator.
• −Active herpes zoster infection within 2 months prior to the screening visit.
• −Any medical condition that promotes suicidal attempt or behavior within 6 months prior to the screening visit and in the opinion of the investigator might interfere with subject's participation in the study or is a risk for a suicide attempt.
• −History of unstable or severe cardiac, pulmonary, oncological, hepatic, or renal disease or active cancer or another medically significant illness other than Amyotrophic lateral sclerosis, precluding safe participation of subject in this study in the opinion of the investigator.
• −Subjects who have taken concomitant medications that are substrates of drug metaboliz-ing enzymes (Cytochrome P450 1A2 and/or Cytochrome P450 2B6) within 7 days or 5 half-lives of the medication (whichever is longer) before the first dose of Investigational product and throughout the study.
• −Use of any steroids, colchicine, or anti-IL-1 inhibitors within 7 days or 5 half-lives of the medication (whichever is longer) prior to the first dose of Investigational product administration.
• −Use of any investigational drug concurrently or within 4 weeks or 5 half-lives (whichever is longer) prior to the first dose of Investigational product administration.
• −Any clinically significant condition and/or laboratory significant value that would prevent the subject from participating in the study in the opinion of the investigator.
• −Received a live vaccine within 14 days before the screening visit or planning to receive during the study duration.
• −Subjects who have received stem cell or gene therapy for Amyotrophic lateral sclerosis at any time in the past.
• −Following laboratory test values at screening:
• −Alanine aminotransferase or Aspartate aminotransferase values \>3.0 × Upper Limit of Normal
• −Bilirubin \>1.5 × Upper Limit of Normal unless the subject has documented Gilbert's syndrome (isolated bilirubin \>1.5 × Upper Limit of Normal is acceptable if bilirubin is fractionated, and direct bilirubin is \<35%)
• −Estimated glomerular filtration rate (eGFR) \<60 mL/min/1.73 m2
• −For those participating in the optional Cerebrospinal fluid collection, contraindications to lumbar puncture including but not limited to lumbar scoliosis, coagulopathy, infection at siteTrial siteA hospital or clinic where a study is actually run.Read more → of puncture, or use of anticoagulants.
• −Subjects with history of epilepsy within 6 months of screening visit.
• −Use or intended use of any medications/products known to alter drug absorption, metabolism, or elimination processes, including St. John's Wort, within 4 weeks of screening and up to end of study. Use of such medication will be considered on a case-by-case basis as per the opinion of the investigator and/or independent medical monitor.
• −Receiving an elemental diet or parenteral nutrition.
• −Received blood transfusion within 3 months prior to screening.
• −Inability to be venipunctured or those not able to tolerate venous puncture.
• −Employee of the investigator or study site, with direct involvement in the proposed study or other studies under the direction of that investigator or study site, as well as family members of employees of investigator or the investigator.
• −Any condition not mentioned in any of above criteria that, as per the investigator, would hinder participation of the subject in the study. This may include, but not limited to, considerations of safety, compliance, or other factors that could impact the integrity of the study or the well-being of the subject.
• −For Open LabelOpen-labelEveryone knows which treatment is being given — nothing is hidden.Read more → Extension
• −Inclusion CriteriaInclusion criteriaThe things you must have or be for a study to consider you.Read more →:
• −Completion in the randomizedRandomisedWhich group you go into is decided by chance, not by you or your doctor.Read more →, double blindDouble-blindNeither you nor the study team knows which group you are in.Read more → Usnoflast study (main study).
• −Subjects who elect to continue treatment after completion of Usnoflast phase 2b study must enrol in the OLE within 28 days of the completion of Week 36 visit of the main study.
• −Provide a new informed consent to enter the OLE phase.
• −Exclusion CriteriaExclusion criteriaThe things that would prevent someone from taking part.Read more →:
• −Discontinued IP prematurely in the double-blind phase of the study for reasons other than tracheostomy or permanent-assisted ventilation.
• −Treatment with or use of any restricted medications.
• −Any ongoing AEAdverse eventAny medical problem that happens during a study, whether or not the treatment caused it.Read more → that, in the opinion of the site investigator, is clear contraindication to the IP.
• −Unstable cardiac or other life-threatening disease emergent during the randomized, double-blind study
• −Any major medical history or other evidence of severe illness or any other conditions that would make the subject, in the opinion of the investigator, unsuitable for the study.
• −If female, breastfeeding, known to be pregnant, planning to become pregnant during the study, or of child-bearing potential and unwilling to use effective contraception during the study and for at least 1 month after administration of last dose of Investigational product. If male of reproductive capacity, unwilling to use effective contraception during the study and for at least 1 month after administration of last dose of Investigational product.
• −If female, breastfeeding, known to be pregnant, planning to become pregnant during the study, or of child-bearing potential and unwilling to use effective contraception during the study and for at least 1 month after administration of last dose of IP. If male of reproductive capacity, unwilling to use effective contraception during the study and for at least 1 month after administration of last dose of IP.
• −Surgery within last 3 months or planned major surgery within next 3 months from the date of screening (other than minor cosmetic surgery and minor dental surgery).